Wanted: Clinical Research Associate

Upsilon Global; Brusque; Presencial; BRL 120 000 - 180 000; Tempo integral

Resumo da oferta

Upsilon Global is seeking a Freelance Clinical Research Associate (CRA) in Brazil to support an infectious disease clinical trial. The role focuses on site monitoring, regulatory compliance, and collaboration with international teams.

The ideal candidate has CRA experience in clinical trials, strong knowledge of ICH-GCP, and is fluent in Portuguese and English. They should be available for freelance/contract work and ideally based in Brazil.

Qualificações

• Must have prior CRA experience in clinical trials.
• Experience with site monitoring and clinical trial activities.
• Strong understanding of ICH-GCP and clinical research processes.
• Fluent in Portuguese and English.
• Ideally based in Brazil and available for freelance/contract work.
• Infectious disease experience is advantageous.

Responsabilidades

• Monitor clinical sites and oversee trial activities.
• Ensure adherence to protocol, GCP, and regulatory requirements.
• Collaborate with sponsors, sites, and data management teams.

Conhecimentos

Site Monitoring

Clinical Trials

ICH-GCP

Portuguese

English

Descrição da oferta de emprego

Join a growing international CRO and take the next step in your Clinical Research career.

We are looking for a Freelance Clinical Research Associate (CRA) in Brazil to support an exciting Infectious Disease clinical trial.

Our client is an international CRO supporting clinical research programs across a range of therapeutic areas, with a strong focus on scientific expertise, collaboration, and high-quality clinical delivery.

This is a great opportunity for a CRA looking to gain further experience within an international environment, and we are particularly interested in speaking with professionals who may be considering their first freelance/contract opportunity.

We do not need previous freelance experience — if you have a solid foundation as a CRA and are looking to make the move into contracting, we would be very interested in speaking with you.

Key Requirements:

• Previous experience working as a CRA within clinical trials
• Experience with site monitoring and clinical trial activities
• Strong understanding of ICH-GCP and clinical research processes
• Fluent in Portuguese and English
• Ideally based in Brazil
• Available to work on a freelance/contract basis
• Previous Infectious Disease experience would be advantageous